LUTECH Multi-parameter Patient Monitor - Indonesia BPOM Medical Device Registration
LUTECH Multi-parameter Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502122172. The device is manufactured by LUTECH INDUSTRIES, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GAMAMED.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUTECH INDUSTRIES, INCCountry of Origin
United States
Authorized Representative
GAMAMEDAR Address
JL. WR. SUPRATMAN 56 B
Registration Date
Apr 16, 2021
Expiry Date
Dec 31, 2023
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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